Quality Documentation Optimization
Quality Documentation Optimization ResourceResponsibilities Observation aggregationTraining/process insight, and stage-gate visibilityGather observations from Manufacturing and Quality reviewConvert themes into training/process recommendationsBuild cycle-time and stage-gate visibilityPrepare sustainment tools for leadership governance.Requirements 5-10+ years of Quality Manufacturing experience within pharma industry8 week contract opportunity; full-time weekly hours; onsite in Memphis, TN